Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
Disease Name
Chondroblastoma
Standard Disease Name
chondroblastoma
MeSH Tree
No data
ICD-10
No data
Identifiers
DO ID
No data
MeSH ID
D002804
OMIM ID
No data
UMLS ID
C0008441
HPO ID
No data
Description and Extensions
Description
NCI2016_02D:A benign, chondroid-producing, well-circumscribed, lytic neoplasm usually arising from the epiphysis of long bones. It is characterized by the presence of chondroblasts, osteoclast-like giant cells, chondroid formation, calcification, and mitotic activity. In aggressive cases, there is rearrangement of the 8q21 chromosome band. It occurs most frequently in children and young adults and rarely metastasizes.|MSH2017_2016_08_12:A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. It occurs primarily in the epiphyses of adolescents. It is relatively rare and represents less than 2% of all primary bone tumors. The peak incidence is in the second decade of life; it is about twice as common in males as in females. (From Dorland, 27th ed; Holland et al., Cancer Medicine, 3d ed, p1846)|HPO2016_07_04:A usually benign tumor composed of cells which arise from chondroblasts or their precursors and which tend to differentiate into cartilage cells. [HPO:probinson, pmid:19387641]
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